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DE69420053D1 - NEUROPROTECTIVE CHROMAN CONNECTIONS - Google Patents

NEUROPROTECTIVE CHROMAN CONNECTIONS

Info

Publication number
DE69420053D1
DE69420053D1 DE69420053T DE69420053T DE69420053D1 DE 69420053 D1 DE69420053 D1 DE 69420053D1 DE 69420053 T DE69420053 T DE 69420053T DE 69420053 T DE69420053 T DE 69420053T DE 69420053 D1 DE69420053 D1 DE 69420053D1
Authority
DE
Germany
Prior art keywords
pct
chroman
neuroprotective
connections
sec
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
DE69420053T
Other languages
German (de)
Other versions
DE69420053T2 (en
Inventor
Todd Butler
Bertrand Chenard
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Corp Belgium
Pfizer Inc
Original Assignee
Pfizer Corp Belgium
Pfizer Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Corp Belgium, Pfizer Inc filed Critical Pfizer Corp Belgium
Application granted granted Critical
Publication of DE69420053D1 publication Critical patent/DE69420053D1/en
Publication of DE69420053T2 publication Critical patent/DE69420053T2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • A61P39/02—Antidotes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Anesthesiology (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Toxicology (AREA)
  • Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cosmetics (AREA)
  • Saccharide Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

PCT No. PCT/IB94/00365 Sec. 371 Date Oct. 24, 1996 Sec. 102(e) Date Oct. 24, 1996 PCT Filed Nov. 21, 1994 PCT Pub. No. WO95/20587 PCT Pub. Date Aug. 3, 19953R*4S*3-[4-(4-fluorophenyl)-4-hydroxy-piperidin-1-yl]-chroman-4,7-diol, its enantiomers and pharmaceutically acceptable salts are effective oral agents for treating diseases and conditions susceptible to treatment by NMDA blocking drugs.
DE69420053T 1994-01-31 1994-11-21 NEUROPROTECTIVE CHROMAN CONNECTIONS Expired - Fee Related DE69420053T2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US18947994A 1994-01-31 1994-01-31
PCT/IB1994/000365 WO1995020587A1 (en) 1994-01-31 1994-11-21 Neuroprotective chroman compounds

Publications (2)

Publication Number Publication Date
DE69420053D1 true DE69420053D1 (en) 1999-09-16
DE69420053T2 DE69420053T2 (en) 1999-11-25

Family

ID=22697514

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69420053T Expired - Fee Related DE69420053T2 (en) 1994-01-31 1994-11-21 NEUROPROTECTIVE CHROMAN CONNECTIONS

Country Status (27)

Country Link
US (1) US5744483A (en)
EP (1) EP0741724B1 (en)
JP (1) JP2866743B2 (en)
CN (1) CN1048247C (en)
AT (1) ATE183184T1 (en)
AU (1) AU684568B2 (en)
BR (2) BR9408506A (en)
CA (1) CA2182101C (en)
CO (1) CO4230161A1 (en)
CZ (1) CZ286757B6 (en)
DE (1) DE69420053T2 (en)
DK (1) DK0741724T3 (en)
EG (1) EG20672A (en)
ES (1) ES2134361T3 (en)
FI (1) FI113769B (en)
GR (1) GR3031356T3 (en)
HU (1) HU221633B1 (en)
IL (1) IL112415A (en)
MY (1) MY111623A (en)
NO (1) NO309190B1 (en)
NZ (1) NZ275151A (en)
PE (1) PE43795A1 (en)
PL (1) PL179448B1 (en)
RU (1) RU2126404C1 (en)
TW (1) TW449591B (en)
WO (1) WO1995020587A1 (en)
ZA (1) ZA95692B (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997010240A1 (en) * 1995-09-15 1997-03-20 Pfizer Inc. Phenol derivatives with pharmaceutical activity
TW498067B (en) * 1996-07-19 2002-08-11 Hoffmann La Roche 4-hydroxy-piperidine derivatives
UA73981C2 (en) * 2000-03-10 2005-10-17 Merck Patent Gmbh (r)-(-)-2-[5-(4-fluorophenyl)-3-pyridylmethylaminomethyl]-chromane for treatment of extrapyramidal movement disorders (variants), pharmaceutical composition and kit
US6407235B1 (en) * 2000-08-21 2002-06-18 Hoffmann-La Roche Inc. Prodrug acid esters of [2-(4-benzyl-3-hydroxy-piperidin-1-yl)-ethansulfonyl]phenol
ZA200108038B (en) * 2000-10-02 2003-04-01 Pfizer Prod Inc Prophylactic use of n-methyl-d-asparrate (NMDA) antagonists.
EP1674087A1 (en) 2000-10-02 2006-06-28 Pfizer Products Inc. Prophylactic use of n-methyl-d-aspartate (NMDA) antagonists
SE0100902D0 (en) 2001-03-15 2001-03-15 Astrazeneca Ab Compounds
ATE352302T1 (en) * 2001-07-26 2007-02-15 Merck Patent Gmbh USE OF 2- 5-(4-FLUOROPHENYL)-3-PYRIDYLMETHYLAMINOMETHYL CHROMANE AND ITS PHYSIOLOGICALLY ACCEPTABLE SALTS
RU2240113C1 (en) * 2003-01-23 2004-11-20 Государственное образовательное учреждение высшего профессионального образования Московская медицинская академия им. И.М.Сеченова Method for urgent medicinal aid at acute trauma of spinal cord
US7671072B2 (en) * 2003-11-26 2010-03-02 Pfizer Inc. Aminopyrazole derivatives as GSK-3 inhibitors
ATE499355T1 (en) 2005-11-03 2011-03-15 Hoffmann La Roche ARYLSULFONYL CHROMANS AS 5-HT6 INHIBITORS
MX2008009414A (en) * 2006-01-20 2008-10-01 Schering Corp Carbocyclic and heterocyclic arylsulfones as gamma secretase inhibitors.
RU2418578C1 (en) * 2009-12-08 2011-05-20 Новосибирский институт органической химии им. Н.Н. Ворожцова Сибирского отделения Российской академии наук (НИОХ СО РАН) APPLICATION OF 4,7-DIMETHYL-2-(PROP-1-ENYL)-3,4,4a,5,8,8a-HEAHYDRO-2H-CHROMEN-4,8-DIOL AS ANALGESIC
EP2522647B1 (en) * 2011-05-10 2014-04-30 DSM IP Assets B.V. Process of separating chiral isomers of chroman compounds and their derivatives and precursors

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3294804A (en) * 1961-01-27 1966-12-27 Sterling Drug Inc 1-(3-hydroxy-3-phenylpropyl)-4-phenyl-4-propionoxy-piperidine
FR5733M (en) * 1966-09-27 1968-01-22
GB1495526A (en) * 1974-05-31 1977-12-21 Beecham Group Ltd Chroman derivatives
US4016281A (en) * 1975-02-22 1977-04-05 Merck Patent Gesellschaft Mit Beschrankter Haftung Tetralone and indanone compounds
US4082755A (en) * 1977-02-14 1978-04-04 Janssen Pharmaceutica N.V. 1-[(Diarylmethyl)aminoalkyl]piperidimes
WO1980000152A1 (en) * 1978-07-03 1980-02-07 Sandoz Ag 3-aminopropoxy-aryl derivates,preparation and use thereof
US4358456A (en) * 1980-05-03 1982-11-09 John Wyeth & Brother Limited Antipsychotic piperidinomethyl-indole derivatives
DE3045688A1 (en) * 1980-12-04 1982-07-08 C.H. Boehringer Sohn, 6507 Ingelheim NEW 8-ARYLALKYL-3-PHENYL-3-NORTROPANOLE, THE ACID ADDITION SALTS THEREOF, THE MEDICINAL PRODUCTS CONTAINING THE SAME AND METHOD FOR THE PRODUCTION THEREOF
GB2107706A (en) * 1981-09-25 1983-05-05 Beecham Group Plc Benzopyrans
EP0093534A1 (en) * 1982-04-28 1983-11-09 Beecham Group Plc Novel chromanols
ES523609A0 (en) * 1982-07-05 1985-03-01 Erba Farmitalia PROCEDURE FOR PREPARING N-IMIDAZOLYLIC DERIVATIVES OF BICYCLE COMPOUNDS.
GB8308064D0 (en) * 1983-03-24 1983-05-05 Beecham Group Plc Active compounds
FR2546166B1 (en) * 1983-05-19 1985-10-25 Synthelabo ENANTIOMERS OF ERYTHRO (BENZYL-4 PIPERIDINO) -2 (HYDROXY-4 OR BENZYLOXY-4 PHENYL) -1 PROPANOL, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
FR2581993B1 (en) * 1985-05-14 1988-03-18 Synthelabo (BENZOYL-4 PIPERIDINO) -2 PHENYL-1 ALCANOLS DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
US4957928A (en) * 1986-06-26 1990-09-18 Ciba-Geigy Corporation Hydrogenated 1-benzooxacycloalkylpyridinecarboxylic acid compounds
US4968678A (en) * 1988-02-19 1990-11-06 Eli Lilly And Company Tetrazole excitatory amino acid receptor antagonists
FR2640266B2 (en) * 1988-07-12 1992-07-10 Synthelabo INDOLONES-2, QUINOLEINONES-2, BENZO (B) AZEPINONES-2 AND BENZIMIDAZOLONES-2 DERIVATIVES OF (HYDROXY-1 PIPERIDINYL-2 ALKYL), THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
US4968878A (en) * 1989-02-07 1990-11-06 Transitions Research Corporation Dual bumper-light curtain obstacle detection sensor
US4902695A (en) * 1989-02-13 1990-02-20 Eli Lilly And Company Excitatory amino acid receptor antagonists
WO1990014087A1 (en) * 1989-05-17 1990-11-29 Pfizer Inc. 2-piperidino-1-alkanol derivatives as antiischemic agents
MX24433A (en) * 1990-02-06 1993-05-01 Pfizer DERIVATIVES OF 3-PIPERIDINE-1-CHROMANOL AND ITS ANALOGS AND PROCEDURE FOR THE PREPARATION
US5192751A (en) * 1992-07-24 1993-03-09 Eli Lilly And Company Use of competitive NMDA receptor antagonists in the treatment of urinary incontinence

Also Published As

Publication number Publication date
NO309190B1 (en) 2000-12-27
DE69420053T2 (en) 1999-11-25
NO963186L (en) 1996-07-30
EP0741724A1 (en) 1996-11-13
WO1995020587A1 (en) 1995-08-03
CN1048247C (en) 2000-01-12
RU2126404C1 (en) 1999-02-20
US5744483A (en) 1998-04-28
DK0741724T3 (en) 1999-12-20
AU8066394A (en) 1995-08-15
CO4230161A1 (en) 1995-10-19
IL112415A (en) 1999-07-14
EP0741724B1 (en) 1999-08-11
CA2182101A1 (en) 1995-08-03
IL112415A0 (en) 1995-03-30
ZA95692B (en) 1996-07-30
FI950403A0 (en) 1995-01-30
NO963186D0 (en) 1996-07-30
GR3031356T3 (en) 2000-01-31
TW449591B (en) 2001-08-11
CN1142825A (en) 1997-02-12
EG20672A (en) 1999-11-30
AU684568B2 (en) 1997-12-18
BR9408506A (en) 1997-08-05
BR9500380A (en) 1995-10-17
JP2866743B2 (en) 1999-03-08
PL315681A1 (en) 1996-11-25
CA2182101C (en) 1999-08-03
PE43795A1 (en) 1995-12-09
FI113769B (en) 2004-06-15
MY111623A (en) 2000-09-27
ATE183184T1 (en) 1999-08-15
FI950403L (en) 1995-08-01
HU221633B1 (en) 2002-12-28
ES2134361T3 (en) 1999-10-01
CZ225696A3 (en) 1997-01-15
CZ286757B6 (en) 2000-06-14
HUT75942A (en) 1997-05-28
HU9602100D0 (en) 1996-09-30
PL179448B1 (en) 2000-09-29
JPH09501698A (en) 1997-02-18
NZ275151A (en) 1998-02-26

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Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee